Job Description
- To prepare and review documents for manufacturing activities which includes but not limited to master batch records, SOPs, change controls, master packaging specifications and other manufacturing related documents.
- Co-ordination and communication on routinely basis with US team.
- Updation of required status and database for operations and Tech services work flow.
- To work in collaboration with team members to create the highest quality documents and timely delivery of outputs consistently.
- Prepare process validation protocols & reports for manufacturing process and cleaning process qualification; data analysis and prepare reports.
- Initiation of Change Controls, Deviations and CAPAs as and when required.
Qualifications
Experience - 3-5yrs
Qualification - Bpharm / Mpharm
About Us
Amneal is an equal opportunity employer. We do not discriminate based on caste, religion, gender, disability, or any other legally protected status. We believe in fostering a workplace that values diversity and inclusion.
